Thomas Martin G, Marwood Roxanne M, Parsons Anna E, Parsons Richard B
King's College London, Institute of Pharmaceutical Science, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, United Kingdom.
King's College London, Institute of Pharmaceutical Science, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, United Kingdom.
Toxicol In Vitro. 2015 Dec 25;30(1 Pt B):300-8. doi: 10.1016/j.tiv.2015.10.007. Epub 2015 Oct 21.
The lactate dehydrogenase (LDH) assay is a commonly-used tool for assessing toxicity in vitro. However, anecdotal reports suggest that foetal bovine serum (FBS) may contain LDH at concentrations significant enough to interfere with the assay and thus reduce its sensitivity. A series of experiments were performed to determine whether addition of FBS to culture medium significantly elevated culture media LDH content, and whether replacement of FBS with heat inactivated foetal bovine serum (HI-FBS) reduced LDH content and interfered with cell response to cytotoxic challenge. The addition of FBS at 5, 10 and 15% final concentrations increased culture medium LDH content in a dose-dependent manner. The substitution of HI-FBS for FBS reduced culture medium LDH content and increased the dynamic range of the assay. Cell viability of the SH-SY5Y human neuroblastoma and N27 rat mesencephalic neurone cell lines were significantly reduced as measured using the MTT reduction assay, whilst HI-FBS only affected toxicity response in a cell- and toxin-specific manner, although these effects were small. Hence, for cell lines with a high FBS requirement, the use of HI-FBS or alternative toxicity assays can be considered, or the use of alternative formulations, such as chemically-defined serum-free media, be adopted.
乳酸脱氢酶(LDH)测定是一种常用的体外毒性评估工具。然而,有传闻称胎牛血清(FBS)中可能含有浓度足以干扰该测定从而降低其灵敏度的LDH。进行了一系列实验,以确定向培养基中添加FBS是否会显著提高培养基中LDH的含量,以及用热灭活胎牛血清(HI-FBS)替代FBS是否会降低LDH含量并干扰细胞对细胞毒性攻击的反应。最终浓度为5%、10%和15%的FBS添加量以剂量依赖的方式增加了培养基中LDH的含量。用HI-FBS替代FBS降低了培养基中LDH的含量,并增加了该测定的动态范围。使用MTT还原测定法测量时,SH-SY5Y人神经母细胞瘤和N27大鼠中脑神经元细胞系的细胞活力显著降低,而HI-FBS仅以细胞和毒素特异性方式影响毒性反应,尽管这些影响较小。因此对于对FBS需求较高的细胞系,可以考虑使用HI-FBS或替代毒性测定法,或者采用替代配方,如化学成分明确的无血清培养基。